absent midgut Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the portion of the embryonic gut between the foregut and the hindgut (Mammalian Phenotype Ontology, MP_0009706)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009706
Similar Terms
Downloads & Tools

Genes

3 gene mutations causing the absent midgut phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXF1 forkhead box F1
FURIN furin (paired basic amino acid cleaving enzyme)
RUNX1T1 runt-related transcription factor 1; translocated to, 1 (cyclin D-related)